All variants in the WWOX gene

Information The variants shown are described using the NM_016373.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-/. - c.293C>T r.(?) p.(Pro98Leu) - benign g.78148935C>T g.78115038C>T WWOX(NM_016373.4):c.293C>T (p.P98L) - WWOX_000015 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-/. - c.293C>T r.(?) p.(Pro98Leu) - benign g.78148935C>T g.78115038C>T - - WWOX_000015 25 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs144601717 Germline - 25/2795 individuals - 0 - Mohammed Faruq
-/. - c.293C>T r.(?) p.(Pro98Leu) - benign g.78148935C>T g.78115038C>T - - WWOX_000015 1 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs144601717 Germline - 1/2795 individuals - 0 - Mohammed Faruq
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